| Literature DB >> 29209573 |
Abhishek D Garg1, Sanket More1, Nicole Rufo1, Odeta Mece1, Maria Livia Sassano1, Patrizia Agostinis1, Laurence Zitvogel2,3,4,5, Guido Kroemer6,7,8,9,10,11,12, Lorenzo Galluzzi6,13,14.
Abstract
The expression "immunogenic cell death" (ICD) refers to a functionally unique form of cell death that facilitates (instead of suppressing) a T cell-dependent immune response specific for dead cell-derived antigens. ICD critically relies on the activation of adaptive responses in dying cells, culminating with the exposure or secretion of immunostimulatory molecules commonly referred to as "damage-associated molecular patterns". Only a few agents can elicit bona fide ICD, including some clinically established chemotherapeutics such as doxorubicin, epirubicin, idarubicin, mitoxantrone, bleomycin, bortezomib, cyclophosphamide and oxaliplatin. In this Trial Watch, we discuss recent progress on the development of ICD-inducing chemotherapeutic regimens, focusing on studies that evaluate clinical efficacy in conjunction with immunological biomarkers.Entities:
Keywords: antigen-presenting cell; autophagy; cytotoxic T lymphocyte; damage-associated molecular pattern; dendritic cell; endoplasmic reticulum stress; immune checkpoint blocker; type I interferon
Year: 2017 PMID: 29209573 PMCID: PMC5706600 DOI: 10.1080/2162402X.2017.1386829
Source DB: PubMed Journal: Oncoimmunology ISSN: 2162-4011 Impact factor: 8.110